Evidence map›Paper›PMID 21642413›Full record

ArticleApplied and environmental microbiology2011

Potentially human-pathogenic Escherichia coli O26 in Norwegian sheep flocks.

C Sekse, M Sunde, B-A Lindstedt, P Hopp, T Bruheim, K S Cudjoe, B Kvitle, A M Urdahl

Abstract read
In one paragraph

Article in Applied and environmental microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

C SekseNorwegian Veterinary Institute, Oslo, Norway.
M Sunde
B-A Lindstedt
P Hopp
T Bruheim
K S Cudjoe
B Kvitle
A M Urdahl

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A national survey of Escherichia coli O26 in Norwegian sheep flocks was conducted, using fecal samples to determine the prevalence. In total, 491 flocks were tested, and E. coli O26 was detected in 17.9% of the flocks. One hundred forty-two E. coli O26 isolates were examined for flagellar antigens (H typing) and four virulence genes, including stx and eae, to identify possible Shiga toxin-producing E. coli (STEC) and enteropathogenic E. coli (EPEC). Most isolates (129 out of 142) were identified as E. coli O26:H11. They possessed eae and may have potential as human pathogens, although only a small fraction were identified as STEC O26:H11, giving a prevalence in sheep flocks of only 0.8%. Correspondingly, the sheep flock prevalence of atypical EPEC (aEPEC) O26:H11 was surprisingly high (15.9%). The genetic relationship between the E. coli O26:H11 isolates was investigated by pulsed-field gel electrophoresis (PFGE) and multilocus variable number tandem repeat analysis (MLVA), identifying 63 distinct PFGE profiles and 22 MLVA profiles. Although the MLVA protocol was less discriminatory than PFGE and a few cases of disagreement were observed, comparison by partition mapping showed an overall good accordance between the two methods. A close relationship between a few isolates of aEPEC O26:H11 and STEC O26:H11 was identified, but all the E. coli O26:H11 isolates should be considered potentially pathogenic to humans. The present study consisted of a representative sampling of sheep flocks from all parts of Norway. This is the first large survey of sheep flocks focusing on E. coli O26 in general, including results of STEC, aEPEC, and nonpathogenic isolates.

Indexed as

AnimalsAntigens, BacterialBacterial Typing TechniquesElectrophoresis, Gel, Pulsed-FieldEnteropathogenic Escherichia coliEscherichia coli InfectionsEscherichia coli ProteinsFecesMultilocus Sequence TypingNorwayO AntigensSerotypingSheepSheep DiseasesShiga ToxinVirulence FactorsAntigens, BacterialEscherichia coli ProteinsH antigenO AntigensShiga ToxinVirulence Factors

Identifiers

PMID21642413
PMCPMC3147382

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.